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OKYO Pharma to Present at International Tear Film and Ocular Surface Society Conference London and New York, NY

Key Takeaway: OKYO Pharma Limited is set to present at the 10th International Tear Film & Ocular Surface Society Conference in Venice from October 30 to November 2, 2024. The company will share results from its recent Phase 2 trial of OK-101, aimed at treating dry eye disease and neuropathic corneal pain. CEO Dr. Gary S. Jacob emphasized the importance of finding lasting treatments for patients suffering from these debilitating conditions. The conference will feature one-on-one discussions regarding the clinical findings and ongoing studies at Tufts Medical Center.

Market Sentiment Analysis

POSITIVE FACTORS

  • OKYO Pharma is presenting at a prestigious international conference.
  • Successful Phase 2 trial results indicate potential for effective treatments.
  • The company is focused on addressing severe ocular conditions with no approved therapies.

Full Press Release Details

Pharma to Present at International Tear Film and Ocular Surface Society Conference
and New York, NY, October 30, 2024. OKYO Pharma Limited (NASDAQ: OKYO), a clinical-stage biopharmaceutical company developing innovative
therapies for the treatment of neuropathic corneal pain (NCP), a severe ocular condition without an FDA approved therapy, and for inflammatory
dry eye disease (DED), a multi-billion-dollar market, is pleased to announce that it will be presenting at the 10th International Tear
Film & Ocular Surface Society Conference in Venice, Italy during October 30 - November 2, 2024. The OKYO management team will be
participating in one-on-one meetings to discuss the dry eye disease trial results, and also the recent opening of our Phase 2 trial of
OK-101 to treat patients with Neuropathic Corneal Pain at Tufts Medical Center, Boston, Massachusetts, USA.
Tear Film and Ocular Surface Society (TFOS) Conference
Title: Efficacy and Safety Results of First-in-Human Phase 2 Trial of OK-101 in Dry Eye Patients
By: Raj Patil, Ph.D., Chief Scientific Officer of OKYO Pharma
of Presentation: Saturday, November 2, 2024
Details: Poster Session III
are thrilled to share our clinical findings with the TFOS community," said Dr. Gary S. Jacob, Ph.D., CEO of OKYO Pharma. "Dry
Eye Disease is a multifactorial and often frustrating condition for both patients and eye care providers, and our goal is to provide
an effective, long-lasting treatment that improves the quality of life for millions who struggle with DED daily."
further information on the ongoing Phase 2 trial of OK-101 to treat Neuropathic Corneal Pain, or to inquire about participation, please
Dry Eye Disease (DED)
is a common condition that occurs when one's tears are unable to adequately lubricate the eyes. This condition affects approximately
49 million people in the United States alone and has been difficult to positively diagnose and treat due to the multifactorial nature
of the condition. Several contributing factors can lead to this condition, including age, sex, certain medical conditions, reduced tear
production and tear film dysfunction.
corneal pain (NCP) is a condition that causes pain and sensitivity of the eyes, face, or head. The exact cause of NCP is unknown but
thought to result from nerve damage to the cornea combined with inflammation. NCP, which can exhibit as a severe, chronic, or debilitating
condition in patients suffering from a host of ophthalmic conditions, is presently treated by various topical and systemic treatments
in an off-label fashion. There are no approved commercial treatments currently available for this condition.
is a lipid conjugated chemerin peptide agonist of the ChemR23 G-protein coupled receptor which is typically found on immune cells of
the eye responsible for the inflammatory response. OK-101 was developed using a membrane-anchored-peptide technology to produce a novel
long-acting drug candidate for treating dry eye disease. OK-101 has been shown to produce anti-inflammatory and pain-reducing activities
in mouse models of dry eye disease and corneal neuropathic pain (NCP), respectively, and is designed to combat washout through the inclusion
of the lipid anchor built into the drug molecule to enhance the residence time of OK-101 within the ocular environment. OK-101 showed
clear statistical significance in multiple endpoints in a recently completed Phase 2, multi-center, double-masked, placebo-controlled
trial of OK-101 to treat DED, and is presently being evaluated in a randomized, placebo-controlled,
double-masked Phase 2 trial to treat 48 NCP patients.
Pharma Limited (NASDAQ: OKYO) is a clinical stage biopharmaceutical company developing innovative therapies for the treatment of NCP
and DED, with ordinary shares listed for trading on the NASDAQ Capital Market. OKYO is focused on the discovery and development of novel
molecules to treat NCP and inflammatory DED. In addition to the recently completed Phase 2 trial of OK-101 to treat DED patients, OKYO
is also evaluating OK-101 to treat NCP patients with the just announced opening of a Phase 2 trial to treat the debilitating conditions
of NCP. For further information, please visit www.okyopharma.com.
statements made in this announcement are forward-looking statements. These forward-looking statements are not historical facts but rather
are based on the Company's current expectations, estimates, and projections about its industry, its beliefs, and assumptions. Words
such as anticipates,' expects,' intends,' plans,' believes,' seeks,'
estimates,' and similar expressions are intended to identify forward-looking statements. These statements are not guarantees
of future performance and are subject to known and unknown risks, uncertainties, and other factors, some of which are beyond the Company's
control, are difficult to predict, and could cause actual results to differ materially from those expressed or forecasted in the forward-looking
statements. These and additional risks and uncertainties are described more fully in the company's filings with the SEC, including
those factors identified as "Risk Factors" in our most recent Annual Report on Form 20-F, for the fiscal year ended March
31, 2024. The Company cautions security holders and prospective security holders not to place undue reliance on these forward-looking
statements, which reflect the view of the Company only as of the date of this announcement. The forward-looking statements made in this
announcement relate only to events as of the date on which the statements are made. The Company will not undertake any obligation to
release publicly any revisions or updates to these forward-looking statements to reflect events, circumstances, or unanticipated events
occurring after the date of this announcement except as required by law or by any appropriate regulatory authority.
OKYO Pharma Limited Gary S. Jacob, Chief Executive Officer 917-497-7560
Business Development & Investor Relations Paul Spencer +44 (0)20 7495 2379

Frequently Asked Questions

What is OKYO Pharma presenting at the TFOS Conference?

OKYO Pharma will present results from the Phase 2 trial of OK-101 for dry eye disease.

Where is the TFOS Conference being held?

The TFOS Conference will take place in Venice, Italy, from October 30 to November 2, 2024.

What conditions does OKYO Pharma aim to treat?

OKYO Pharma focuses on treating neuropathic corneal pain and inflammatory dry eye disease.

How many people are affected by dry eye disease in the U.S.?

Approximately 49 million people in the United States suffer from dry eye disease.

What is the role of OK-101?

OK-101 is designed to reduce inflammation and pain in dry eye disease and neuropathic corneal pain.

Last updated: Oct 30, 2024